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- ATPMB
- ATPSB
- MGC5231
- ATP synthase, H+
transporting, mitochondrial F1 complex, beta polypeptide
- mitochondrial ATP
synthetase, beta subunit
- ATP synthase beta
chain, mitochondrial precursor (EC 3.6.3.14).
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- This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP
synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across
the inner membrane during oxidative phosphorylation. ATP synthase is composed of two
linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning
component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP
synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon)
assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the
other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes
the beta subunit of the catalytic core.
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- Location: 12q13.13
- Orientation: minus strand
- Size: 7,891 bp
- 9 exons
- DNA sequence (Human): NC_000012
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- Mutations and SNPs (According
to HGMD and SNP)
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- Size: 529 amino acids; 56560 Da
- Catalytic activity: ATP + H(2)O + H(+)(In) = ADP +
phosphate + H(+)(Out).
- Subcellular location: Mitochondrial.
- Protein domains
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